Cas 1228646-82-9,ethyl 2-amino-4-(3-bromophenyl)-4,5,6,8-tetrahydro-5-oxothiopyrano[3,4-b]pyran-3-carboxylate

1228646-82-9

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Basic information

Product Name: ethyl 2-amino-4-(3-bromophenyl)-4,5,6,8-tetrahydro-5-oxothiopyrano[3,4-b]pyran-3-carboxylate
Synonyms:
CAS NO:1228646-82-9
Molecular Formula:
Molecular Weight: 410.288
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 2-amino-4-(3-bromophenyl)-4,5,6,8-tetrahydro-5-oxothiopyrano[3,4-b]pyran-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-amino-4-(3-bromophenyl)-4,5,6,8-tetrahydro-5-oxothiopyrano[3,4-b]pyran-3-carboxylate(1228646-82-9)
EPA Substance Registry System: ethyl 2-amino-4-(3-bromophenyl)-4,5,6,8-tetrahydro-5-oxothiopyrano[3,4-b]pyran-3-carboxylate(1228646-82-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1228646-82-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1228646-82-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,6,4 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1228646-82:
(9*1)+(8*2)+(7*2)+(6*8)+(5*6)+(4*4)+(3*6)+(2*8)+(1*2)=169
169 % 10 = 9
So 1228646-82-9 is a valid CAS Registry Number.

1228646-82-9Upstream product

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1228646-82-9Relevant academic research and scientific papers

Design and an efficient synthesis of new thiorotenone derivatives

Yao, Changsheng,Wang, Cuihua,Jiang, Bei,Feng, Xiaodong,Yu, Chenxia,Li, Tuanjie,Tu, Shujiang

supporting information; experimental part, p. 2884 - 2887 (2010/08/05)

A series of novel 4-aryl-thiopyrano[3,4-b]pyran-5-one derivatives were synthesized through an efficient one-pot three-component reaction under solvent-free conditions. This work provides a new series of derivatives of thiorotenone with potential biological activity for biomedical screening.

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